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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047157Generated: October 31, 2026

Hydrochloric Acid → (S)-ethyl 6-bromo-1-(1-(tert-butoxycarbonyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/1047157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-butyl (3S)-3-aminopiperidine-1-carboxylateHCID 1501975—
ReactantEthyl 2-(5-bromo-2-fluoronicotinoyl)-3-(dimethylamino)acrylateHCID 68749333—
SolventDimethylformamideHCID 6228—
Product(S)-ethyl 6-bromo-1-(1-(tert-butoxycarbonyl)piperidin-3-yl)-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylateHCID 6879604575.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

Ethyl 2-(5-bromo-2-fluoronicotinoyl)-3-(dimethylamino)acrylate (Intermediate 3, 2.0 g, 5.79 mmol), (S)-tert-butyl 3-aminopiperidine-1-carboxylate (1.160 g, 5.79 mmol), and potassium carbonate (2.042 g, 7.38 mmol) were combined in DMF (10.0 mL). The reaction mixture was heated at 90° C. for 2 h. The reaction mixture was cooled to 0° C. and 1N HCl was slowly added until pH was 5. The resulting precipitate was collected by filtration, washed with water and dried overnight to yield a light yellow solid (2.10 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569484B2
Source datasetuspto-grants-2013_10
ORD IDord-a2847f7ada994500b35207c8fa8ab258
Source noteuspto-grants-2013_10